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Status |
Public on Nov 30, 2019 |
Title |
scRNA-seq [N709-N517] |
Sample type |
SRA |
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Source name |
colon tumor cells
|
Organism |
Mus musculus |
Characteristics |
strain: ApcMin/+ age: 12 weeks Sex: male tissue: colon cell type: DAPI-Cd31-Cd45-Epcam+Cd24+ cells
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Treatment protocol |
Male ApcMin/+ mice between 10 weeks of age were given 2% (w/v) Dextran sulfate sodium salt (DSS) (MP Biomedicals, #0216011090) in drinking water for 5 days
|
Extracted molecule |
polyA RNA |
Extraction protocol |
DAPI-Cd31-Cd45-Epcam+Cd24+ cells were single-cell sorted. FACS-sorted single cells were subjected to cDNA synthesis using Bead-seq method (DOI:10.1016/j.ab.2014.10.011, DOI:10.1038/s41598-017-04616-6). The processes from the production of cDNA libraries to their amplification and first purification were carried out automatically using a Caliper Zephyr compact liquid handler (Perkin Elmer, CA, USA).
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Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina HiSeq 2500 |
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|
Description |
160120_Hiseq3B_l8_009_Dr_Okamoto_N709-N517_GCTACGCT-GCGTAAGA_L008
|
Data processing |
Basecalling was performed using configureBclToFastq.pl of bcl2fastq version 1.8.4 with the following arguments: --with-failed-reads --no-eamss --use-bases-mask Y*,I8,I8 Reference sequences for mapping were prepared using rsem-prepare-reference of RSEM version 1.2.31 and Bowtie2 version 2.2.9. Reads were filtered and trimmed using prinseq-lite.pl of PRINSEQ version 0.20.4 with the following arguments: -min_len 30 -trim_tail_right 5 -trim_tail_left 5 -min_qual_mean 20 -trim_qual_right 20 -trim_qual_left 20 The processed reads were mapped to the reference sequences and TPM (Transcripts Per Million) were calculated using rsem-calculate-expression of RSEM version 1.2.31 and Bowtie2 version 2.2.9 with the default parameters. Gene TPM values were extracted from TPM columns of RSEM gene result files. Genome_build: GRCm38.p4 Supplementary_files_format_and_content: CSV file including TPM values; The column labels are single cell names, and the row labels are gene IDs.
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Submission date |
Nov 29, 2019 |
Last update date |
Dec 01, 2019 |
Contact name |
Daichi Narushima |
Organization name |
National Cancer Center Research Institute
|
Department |
Department of Bioinformatics
|
Street address |
5-1-1 Tsukiji, Chuo-ku
|
City |
Tokyo |
ZIP/Postal code |
104-0045 |
Country |
Japan |
|
|
Platform ID |
GPL17021 |
Series (1) |
GSE141157 |
PROX1 mediates chemoresistance-associated recurrence via maintenance of quiescent colon cancer stem cells |
|
Relations |
BioSample |
SAMN13427388 |
SRA |
SRX7241530 |